Efficient Synthesis of a C 2 -Symmetric 2,2'-Bipyridine-α,α'-1-t-butyl-diol Ligand by Stereoselective Double Hydrogen Transfer to a 2,2'-Bipyridine-diketone

An efficient and practical method was developed for the synthesis of C -symmetric 2,2'-bipyridine-α,α'-1-t-butyl-diol ligands. The disclosed synthesis involves the Ullmann homocoupling of a keto bromo-pyridine under NiCl /Zn/PPh conditions, followed by the stereoselective double hydrogen t...

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Veröffentlicht in:Chemistry : a European journal 2024-10, Vol.30 (56), p.e202402449
Hauptverfasser: Bouzid, Stéphany, Marcoux, Antony, Ollevier, Thierry
Format: Artikel
Sprache:eng
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Zusammenfassung:An efficient and practical method was developed for the synthesis of C -symmetric 2,2'-bipyridine-α,α'-1-t-butyl-diol ligands. The disclosed synthesis involves the Ullmann homocoupling of a keto bromo-pyridine under NiCl /Zn/PPh conditions, followed by the stereoselective double hydrogen transfer to the obtained 2,2'-bipyridine-diketone using Ru Noyori-Ikariya catalysts. This approach allowed the successful synthesis of 2,2'-bipyridine-α,α'-1-t-butyl-diol, i.e (S,S)-Bolm's ligand, with a quantitative yield and an excellent stereoselectivity (ee>99.5 %, de>99.5 %), with an overall yield of 69 % from easily accessible starting materials.
ISSN:1521-3765